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Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants
Ruminants are important for global food security but emit the greenhouse gas methane. Rumen microorganisms break down complex carbohydrates to produce volatile fatty acids and molecular hydrogen. This hydrogen is mainly converted into methane by archaea, but can also be used by hydrogenotrophic acet...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562222/ https://www.ncbi.nlm.nih.gov/pubmed/35931768 http://dx.doi.org/10.1038/s41396-022-01294-9 |
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author | Li, Qiu Shuang Wang, Rong Ma, Zhi Yuan Zhang, Xiu Min Jiao, Jin Zhen Zhang, Zhi Gang Ungerfeld, Emilio M. Yi, Kang Le Zhang, Bai Zhong Long, Liang Long, Yun Tao, Ye Huang, Tao Greening, Chris Tan, Zhi Liang Wang, Min |
author_facet | Li, Qiu Shuang Wang, Rong Ma, Zhi Yuan Zhang, Xiu Min Jiao, Jin Zhen Zhang, Zhi Gang Ungerfeld, Emilio M. Yi, Kang Le Zhang, Bai Zhong Long, Liang Long, Yun Tao, Ye Huang, Tao Greening, Chris Tan, Zhi Liang Wang, Min |
author_sort | Li, Qiu Shuang |
collection | PubMed |
description | Ruminants are important for global food security but emit the greenhouse gas methane. Rumen microorganisms break down complex carbohydrates to produce volatile fatty acids and molecular hydrogen. This hydrogen is mainly converted into methane by archaea, but can also be used by hydrogenotrophic acetogenic and respiratory bacteria to produce useful metabolites. A better mechanistic understanding is needed on how dietary carbohydrates influence hydrogen metabolism and methanogenesis. We profiled the composition, metabolic pathways, and activities of rumen microbiota in 24 beef cattle adapted to either fiber-rich or starch-rich diets. The fiber-rich diet selected for fibrolytic bacteria and methanogens resulting in increased fiber utilization, while the starch-rich diet selected for amylolytic bacteria and lactate utilizers, allowing the maintenance of a healthy rumen and decreasing methane production (p < 0.05). Furthermore, the fiber-rich diet enriched for hydrogenotrophic methanogens and acetogens leading to increased electron-bifurcating [FeFe]-hydrogenases, methanogenic [NiFe]- and [Fe]-hydrogenases and acetyl-CoA synthase, with lower dissolved hydrogen (42%, p < 0.001). In contrast, the starch-rich diet enriched for respiratory hydrogenotrophs with greater hydrogen-producing group B [FeFe]-hydrogenases and respiratory group 1d [NiFe]-hydrogenases. Parallel in vitro experiments showed that the fiber-rich selected microbiome enhanced acetate and butyrate production while decreasing methane production (p < 0.05), suggesting that the enriched hydrogenotrophic acetogens converted some hydrogen that would otherwise be used by methanogenesis. These insights into hydrogen metabolism and methanogenesis improve understanding of energy harvesting strategies, healthy rumen maintenance, and methane mitigation in ruminants. |
format | Online Article Text |
id | pubmed-9562222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95622222022-10-15 Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants Li, Qiu Shuang Wang, Rong Ma, Zhi Yuan Zhang, Xiu Min Jiao, Jin Zhen Zhang, Zhi Gang Ungerfeld, Emilio M. Yi, Kang Le Zhang, Bai Zhong Long, Liang Long, Yun Tao, Ye Huang, Tao Greening, Chris Tan, Zhi Liang Wang, Min ISME J Article Ruminants are important for global food security but emit the greenhouse gas methane. Rumen microorganisms break down complex carbohydrates to produce volatile fatty acids and molecular hydrogen. This hydrogen is mainly converted into methane by archaea, but can also be used by hydrogenotrophic acetogenic and respiratory bacteria to produce useful metabolites. A better mechanistic understanding is needed on how dietary carbohydrates influence hydrogen metabolism and methanogenesis. We profiled the composition, metabolic pathways, and activities of rumen microbiota in 24 beef cattle adapted to either fiber-rich or starch-rich diets. The fiber-rich diet selected for fibrolytic bacteria and methanogens resulting in increased fiber utilization, while the starch-rich diet selected for amylolytic bacteria and lactate utilizers, allowing the maintenance of a healthy rumen and decreasing methane production (p < 0.05). Furthermore, the fiber-rich diet enriched for hydrogenotrophic methanogens and acetogens leading to increased electron-bifurcating [FeFe]-hydrogenases, methanogenic [NiFe]- and [Fe]-hydrogenases and acetyl-CoA synthase, with lower dissolved hydrogen (42%, p < 0.001). In contrast, the starch-rich diet enriched for respiratory hydrogenotrophs with greater hydrogen-producing group B [FeFe]-hydrogenases and respiratory group 1d [NiFe]-hydrogenases. Parallel in vitro experiments showed that the fiber-rich selected microbiome enhanced acetate and butyrate production while decreasing methane production (p < 0.05), suggesting that the enriched hydrogenotrophic acetogens converted some hydrogen that would otherwise be used by methanogenesis. These insights into hydrogen metabolism and methanogenesis improve understanding of energy harvesting strategies, healthy rumen maintenance, and methane mitigation in ruminants. Nature Publishing Group UK 2022-08-05 2022-11 /pmc/articles/PMC9562222/ /pubmed/35931768 http://dx.doi.org/10.1038/s41396-022-01294-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, Qiu Shuang Wang, Rong Ma, Zhi Yuan Zhang, Xiu Min Jiao, Jin Zhen Zhang, Zhi Gang Ungerfeld, Emilio M. Yi, Kang Le Zhang, Bai Zhong Long, Liang Long, Yun Tao, Ye Huang, Tao Greening, Chris Tan, Zhi Liang Wang, Min Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants |
title | Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants |
title_full | Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants |
title_fullStr | Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants |
title_full_unstemmed | Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants |
title_short | Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants |
title_sort | dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562222/ https://www.ncbi.nlm.nih.gov/pubmed/35931768 http://dx.doi.org/10.1038/s41396-022-01294-9 |
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